RELLENO DÉRMICO INYECTABLE
Mexico·Clase III·V. Materiales
quirúrgicos y de
curación·MANDALA MÉXICO LEGAL
AFFAIRS, S.A. DE C.V.·Registered February 07, 2024- Risk Class / Clase de Riesgo
- Clase III
- Product Type (Spanish)
- V. Materiales quirúrgicos y de curación
- Product Type (English)
- V. Materiales quirúrgicos y de curación
- Trade Name (Spanish)
- INBIOTEC AMBER
- Trade Name (English)
- INBIOTEC AMBER
- Analysis ID
- 0400C2024 SSA
- Registration Date
- February 07, 2024
- Name (Spanish)
- MANDALA MÉXICO LEGAL AFFAIRS, S.A. DE C.V.
- Name (English)
- MANDALA MÉXICO LEGAL AFFAIRS, S.A. DE C.V.
Access comprehensive regulatory information for RELLENO DÉRMICO INYECTABLE (RELLENO DÉRMICO INYECTABLE) in the Mexico medical device market through Pure Global AI's free database. This Clase III medical device is registered under COFEPRIS analysis ID 0400C2024 SSA and manufactured by MANDALA MÉXICO LEGAL AFFAIRS, S.A. DE C.V.. The device was registered on February 07, 2024.
This page provides complete registration details including product type (V. Materiales quirúrgicos y de curación), manufacturer information, and regulatory compliance data from the official Mexico COFEPRIS medical device database. Pure Global AI offers free access to Mexico's complete medical device registry with bilingual Spanish/English support, helping global MedTech companies navigate COFEPRIS regulations efficiently.